Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 6
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 6
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs3785356
IL4R
0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs34712979
NPNT
1.000 0.040 4 105897896 splice region variant G/A;T snv 0.17 5
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs3749833
IRF1-AS1
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23 4
rs12123821
LOC112268240 ; FLG-AS1
0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs11071559
RORA
0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4